510(k) K121683 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ACCULIF TL CAGE
| Applicant | Coalign Innovations, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jul 5, 2012 |
| Received | Jun 7, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121683
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.